Spinale arteriovenöse Malformation bei Klippel-Trenaunay-Weber-Syndrom: klinische Verschlechterung nach Lumbalpunktion?

Dietrich, U.; Kloss, T. M.; Bierstedt, T.

doi:10.1055/s-2002-19995

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2005

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“…Die Kombination eines spinalen Angioms mit einem Angiom der Haut im korrespondierenden Dermatom und konsekutiver Hypertrophie der betroffenen Gliedmaße ist typisch für das Klippel-Trenaunay-Weber-Syndrom [2], für das eine Mutation auf Chromosom 5 bekannt ist.…”

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Neurokutane Angiomatose

2005

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A 54-year-old woman developed epilepsy and gait disorder. The initial CCT showed multiple intracerebral cysts. Histologically these turned out to be cavities from repetitive bleedings out of abnormal vessels in the border region. Regular observation during 7 years showed spontaneous episodes of regression and progression of the cysts. In addition, multiple hemangiomas of the skin were found. The case presented here represents an unusual manifestation of neurocutaneous angiomatosis.

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Neurokutane Angiomatose

2005

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Spinale arteriovenöse Malformation bei Klippel-Trenaunay-Weber-Syndrom: klinische Verschlechterung nach Lumbalpunktion?

Cited by 1 publication

References 6 publications

Neurokutane Angiomatose

Neurokutane Angiomatose

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